Canonical Allele Identifier: CA3072749

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125407157C>G , CM000666.2:g.125407157C>G	GRCh38
NC_000004.11:g.126328312C>G , CM000666.1:g.126328312C>G	GRCh37
NC_000004.10:g.126547762C>G	NCBI36
NG_033865.1:g.95746C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001291303.3:c.5569+16C>G MANE Select	NP_001278232.1:n.5569+16C>G
ENST00000394329.9:c.5569+16C>G MANE Select	ENSP00000377862.4:n.5569+16C>G
NM_001291285.1:c.5569+16C>G	NP_001278214.1:n.5569+16C>G
NM_001291285.2:c.5569+16C>G	NP_001278214.1:n.5569+16C>G
NM_001291285.3:c.5569+16C>G	NP_001278214.1:n.5569+16C>G
NM_001291303.1:c.5569+16C>G	NP_001278232.1:n.5569+16C>G
NM_024582.4:c.5569+16C>G	NP_078858.4:n.5569+16C>G
NM_024582.5:c.5569+16C>G	NP_078858.4:n.5569+16C>G
NM_024582.6:c.5569+16C>G	NP_078858.4:n.5569+16C>G
ENST00000335110.5:c.463+16C>G	ENSP00000335169.5:n.463+16C>G
ENST00000394329.7:c.5569+16C>G	ENSP00000377862.3:n.5569+16C>G
ENST00000674496.2:c.340+16C>G	ENSP00000501473.2:n.340+16C>G
XM_011532236.1:c.5569+16C>G	XP_011530538.1:n.5569+16C>G
XM_011532236.2:c.5569+16C>G	XP_011530538.1:n.5569+16C>G
XM_011532237.1:c.340+16C>G	XP_011530539.1:n.340+16C>G
XM_011532237.2:c.340+16C>G	XP_011530539.1:n.340+16C>G